US20160000962A1

US20160000962A1 - Hemostatic Compositions

Info

Publication number: US20160000962A1
Application number: US14/850,101
Authority: US
Inventors: Elisabeth Marianna Wilhelmina Maria Van Dongen
Original assignee: Fujifilm Manufacturing Europe BV
Current assignee: Fujifilm Manufacturing Europe BV
Priority date: 2010-05-20
Filing date: 2015-09-10
Publication date: 2016-01-07
Also published as: WO2011144916A1; DK2571494T3; EP2571494B1; JP2013526564A; JP5914465B2; EP2571494A1; GB201008404D0; US20130066049A1

Abstract

A cross linked recombinant gelatin composition for the induction of blood coagulation and hemostasis.

Description

FIELD OF INVENTION

The present invention is directed to cross-linked gelatin compositions for medical use as a hemostatic agent. The present invention is further directed to the preparation of such compositions. These compositions are useful as hemostatic agents in a variety of medical applications, including vascular plug type devices, wound closure devices, dressings for use to treat incisions, seeping wounds, and the like.

BACKGROUND OF THE INVENTION

Hemostatic agents have a wide range of use from immediate trauma management to use in surgical procedures. These materials help control bleeding from various types of traumas such as open skin wounds and spleen and kidney injuries.
Biodegradable hemostatic agents produced from naturally derived sources have been available for decades. Examples of these are Gelfoam® manufactured by Up-John and disclosed in U.S. Pat. No. 2,465,357; Avitene® manufactured by Acecon and disclosed in U.S. Pat. No. 3,742,955 and Surgicell® manufactured by Johnson and Johnson and disclosed in U.S. Pat. No. 3,364,200. These biodegradable hemostatic agents are primarily formulated using collagen, gelatin and cellulose. Among these materials those made of collagen are the only types known to interact with platelets and activate the clotting cascades to stop bleeding, in a similar way to physiological hemostasis.
Platelets play an important role in the initial stages of hemostasis. Thus, following injury platelets adhere to exposed subendothelial connective tissue; additional platelets then bind to the layer of adhered platelets and form a plug which acts as a barrier to further bleeding. The adhered platelets also release clot-promoting factors and accelerate blood coagulation.
Collagen is a major component of connective tissue and it is well-known that platelets interact with collagen fiber by adhesion and aggregation. In other words, collagen is important in the initiation of hemostasis.
Further improvements on collagen derived hemostatic agents have increased their speed of action. Thus, U.S. Pat. No. 4,215,200 describes chemical modification of collagen fibers to increase the electrostatic charge to a high positive charge at physiological pH. However these treatments introduce the risk of unwanted chemical residues.
Moreover the use of animal-source collagen in hemostatic agents has given rise to safety issues, such as concern over potential immunogenic, e.g., antigenic and allergenic responses. The inability to completely characterize, purify, or reproduce animal-source collagen or gelatin mixtures used currently is of ongoing concern in the pharmaceutical and medical communities. Additional safety concerns exist with respect to bacterial contamination and endotoxin loads resulting from the extraction and purification processes. Recombinantly produced collagen-like peptides or gelatins are a solution to these safety concerns. The use of recombinant collagen-like peptides is disclosed in International Patent Application WO2004078120, however this publication only teaches that material made from recombinant collagen fibrils resembles the microstructure of commercially available hemostatic sponge. International Patent Application WO200009018 teaches the use of a recombinant collagen III in a hemostatis agent. However the recombinant collagen described is also fibrillar in nature due to recombinant production in the presence of a prolyl-4-hydroxylase. The homo- or heterotrimeric configuration mimics native collagen. However homo- or heterotrimeric collagen-like proteins are incompatible with the most efficient recombinant production systems where the proteins are secreted by a micro-organism (especially the preferred Pichia host system). These secretion based systems have many advantages, for example the yield of the secreted recombinant proteins are significantly higher. Another advantage is that downstream processing to purify secreted recombinant proteins is much less elaborate since it does not require disruption of the host-cells to obtain the recombinant product. Therefore, there is need for hemostatic agents based on recombinant collagen-like or gelatin proteins which are effective without requiring chemical modification and easier to produce than the currently known collagen derived agents.

GENERAL DEFINITIONS

The term “comprising” is to be interpreted as specifying the presence of the stated parts, steps or components, but does not exclude the presence of one or more additional parts, steps or components.
Reference to an element by the indefinite article “a” or “an” does not exclude the possibility that more than one of the element is present, unless the context clearly requires that there be one and only one of the elements. The indefinite article “a” or “an” thus usually means “at least one”.
The terms “protein” or “polypeptide” or “peptide” are used interchangeably and refer to molecules consisting of a chain of amino acids, without reference to a specific mode of action, size, three-dimensional structure or origin.
“Gelatin” as used herein refers to any gelatin, whether extracted by traditional methods or recombinant or biosynthetic in origin, or to any molecule having at least one structural and/or functional characteristic of gelatin. Gelatin is currently obtained by extraction from collagen derived from animal (e.g., bovine, porcine, rodent, chicken, equine, piscine) sources, e.g., bones and tissues. The term encompasses both the composition of more than one polypeptide included in a gelatin product, as well as an individual polypeptide contributing to the gelatin material. Thus, the term recombinant gelatin as used in reference to the present invention encompasses both a recombinant gelatin material comprising gelatin polypeptides, as well as an individual gelatin polypeptide. Polypeptides from which gelatin can be derived are polypeptides such as collagens, procollagens, and other polypeptides having at least one structural and/or functional characteristic of collagen. Such a polypeptide could include a single collagen chain, or a collagen homotrimer or heterotrimer, or any fragments, derivatives, oligomers, polymers, or subunits thereof, containing at least one collagenous domain (Gly-X-Y region). The term specifically contemplates engineered sequences not found in nature, such as altered collagen sequences, e.g. a sequence that is altered, through deletions, additions, substitutions, or other changes, from a naturally occurring collagen sequence. Such sequences may be obtained from suitable altered collagen polynucleotide constructs, etc.
A “cross-linking agent” as described herein refers to a composition comprising a cross-linker. “Cross-linker” as used herein refers to a reactive chemical compound that is able to introduce covalent intra- and inter- molecular bridges in organic molecules.

DETAILED DESCRIPTION OF THE INVENTION

The present invention now will be described more fully. However this invention may be embodied in many different forms and should not be construed as limited to the specific embodiments as set forth herein.
The present invention provides a composition comprising a cross-linked gelatin with an isoelectric point of at least 7 for use as a hemostatic agent.
Preferably the gelatin which is to be cross-linked has an isoelectric point of at least 7, more preferably of at least 8, especially of at least 9, more especially of at least 10 and particularly of at least 11 before cross-linking.
Preferably after cross-linking the cross-linked gelatin has an iso-electric point of at least 8, more preferably of at least 9, especially of at least 10, and more especially of at least 11.
The isoelectric point of the gelatin and cross-linked gelatin is calculated based on the amino acid composition of the gelatins.
Preferably the gelatin which is to be cross-linked is a recombinant gelatin. EP 0926543, EP 1014176 and WO 01/34646, and also specifically the examples of EP 0926543 and EP 1014176 all of which are incorporated, in their entirety, herein by reference, describe preferred recombinant gelatins and their production methods, using methylotrophic yeasts, in particular Picha pastoris.
An advantage of recombinant gelatins is that the amino acid sequence can be manipulated to create certain characteristics. Examples of characteristics that can be manipulated are (i) the isoelectric point and charge density of the recombinant gelatin (for example charged amino acids, such as asparagine (Asn), aspartic acid (Asd), glutamine (Gln), glutamic acid (Glu) or lysine (Lys) can be introduced or left out) (ii) the glycosylation pattern (for example the absence of threonine and/or serine amino acids in certain positions results in the absence of glycosylation), (iii) the size of the recombinant gelatin, (iv) the amount of cross-linkable amino acids (for example the amount of lysines), (v) the biodegradability can be amended by the presence or absence of cleavage sites for metalloproteinases.
In a preferred embodiment the gelatin which is to be cross-linked comprises a ratio between the total of arginine and lysine and the total of glutamine and asparagine amino acid residues that is at least 1.0 and more preferably at least 1.1. In a more preferred embodiment, the invention provides a hemostatic composition wherein the gelatin to be cross-linked, preferably a recombinant gelatin, comprises at least 0.40 mmol/g lysine residues before cross-linking, more preferably at least 0.60 mmol/g and especially at least 0.80 mmol/g.
Clearly if more cross-linkable groups are available, the amount of cross-links can in principle be higher if compared to a situation in which less cross-linkable groups are present. Also, the amount of cross-linked groups determine the biodegradability of the cross-linked gelatin. When a recombinant gelatin is used it is possible to control the amount of cross-linkable groups and thus the biodegradability of the cross-linked gelatin can be manipulated.
The optimum degree of cross-linking depends on the intended use of the hemostatic agent and intended method of application. The minimum degree of cross-linking should result in a hemostatic agent that does not dissolve after application.
In another preferred embodiment the recombinant gelatin of the composition is a non-gelling recombinant gelatin with a Bloom strength of below 10 g.
It is also preferred the recombinant gelatin is free of hydroxyproline and hydroxylysine residues. Hydroxylated residues, such as these, allow the formation of intra and extra molecular hydrogen bridges and give rise to the homo or heterotrimeric collagen structures, which are incompatible with the preferred production method via extracellular secretion by a yeast, especially Pichia pastoris. Examples of recombinant gelatins compatible with extracellular secretion are disclosed in EP 0926543, EP 1014176 and WO01/34646.
In a further preferred embodiment functionalized recombinant gelatins for enhanced cell binding and/or with minimal immunogenicity such as, for example, those disclosed in EP 1608681 and EP 1368056 all of which are incorporated, in their entirety, herein by reference, can be cross-linked to form the hemostatic compositions of the invention.
In another preferred embodiment the recombinant gelatines used in the compositions of the present invention have a molecular weight of at least 25 kDa, more preferably of at least 35 kDa and most preferably of at least 50 kDa.
In a further preferred embodiment the recombinant gelatin is a gelatin enriched in RGD motifs. The term ‘RGD-enriched gelatins’ in the context of this invention means that the gelatinous polypeptides have a certain level of RGD motifs, calculated as a percentage of the total number of amino acids per molecule and a more even distribution of RGD motifs. RGD-enriched gelatins in the context of this invention are described in International Patent Applications WO 2004/085473 and WO 2008/103041 which are incorporated herein, in their entirety, by reference. Preferably the recombinant gelatin comprises at least one RGD motif and more preferably at least 3 and especially at least 5 per recombinant gelatin structure.
One or more different gelatins maybe cross-linked. Preferably a single gelatin is cross linked.
An important feature of the cross-linked hemostatic composition of the present invention is that the composition should be biodegradable and so not require invasive surgical methods for its removal.
A priori it is not obvious whether recombinant gelatins will be broken down by the same mechanisms causing degradation of natural gelatins. It is known that natural gelatins and collagens are degraded in the human body by proteases and more specifically matrix-metalloproteinases (MMP). Matrix metalloproteinases (MMP's) are zinc-dependent endopeptidases. The MMP's belong to a larger family of proteases known as the metzincin superfamily. Collectively they are capable of degrading all kinds of extracellular matrix proteins, but also can process a number of bioactive molecules. An important group of MMP's are the collagenases. These MMP's are capable of degrading triple-helical fibrillar collagens into distinctive ¾ and ¼ fragments. These collagens are the major components of bone and cartilage, and MMP's are the only known mammalian enzymes capable of degrading them. Traditionally, the collagenases are: MMP-1 (interstitial collagenase), MMP-8 (neutrophil collagenase), MMP-13 (collagenase 3) and MMP-18 (collagenase 4). Another important group of MMP's is formed by the gelatinases. The main substrates of these MMP's are type IV collagen and gelatin, and these enzymes are distinguished by the presence of an additional domain inserted into the catalytic domain. This gelatin-binding region is positioned immediately before the zinc binding motif, and forms a separate folding unit which does not disrupt the structure of the catalytic domain. The two members of this sub-group are: MMP-2 (72 kDa gelatinase, gelatinase-A) and MMP-9 (92 kDa gelatinase, gelatinase-B). However, International Patent Application WO/2008103045, incorporated herein by reference, discloses that a recombinant gelatin that does not comprise a known cleavage site for MMP was enzymatically degradable by human matrix metalloproteinase 1 (MMP1). Apparently many more types of recombinant gelatin than predicted can be degraded. Therefore the cross-linked recombinant gelatin will exhibit the required gradual biodegradation desirable for a hemostatic composition.
The preparation of the hemostatic composition of the current invention, can be performed by any method known in the art using any cross-linking agent that has a neutral effect on the surface charge, or that introduces positive charges in the cross-linked gelatin.
Preferably the cross-linking agent are carbodiimides such as but not limited to dicyclohexylcarbodiimide, N,N′-diisopropylcarbodiimide and 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide. In a preferred embodiment the method for preparing the hemostatic composition of the current invention is performed by cross-linking the gelatin using a water soluble carbodiimide. In an even more preferred embodiment the gelatin is cross-linked using 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC or EDAC). Cross-linking reaction conditions vary depending on which cross-linking agent is used and would be well known to a skilled person.
A preferred composition the according to the present invention comprises; 92 to 99.9 percent by weight of a cross-linked recombinant gelatin with an iso-electric point of at least 7.
Compositions according to the present invention may be prepared by any method which would be known to the skilled person.
Preferably compositions according to the present invention are prepared by a method which comprises:
(a) dissolving at least 0.1, 0.5, 1, 3, 6, 12, 24 to 35 weight volume percent of gelatin, preferably recombinant gelatin, in water;
(b) lyophilizing the solution;
(c) cross-linking the lyophilized material in a polar solvent, preferably ethanol, comprising a carbodiimide, preferably EDC at a concentration of at least 0.1, 0.25, 0.5, 1, 1.5, 2, 2.5 to 10 weight percent; and cross-linking for at least 10 minutes and up to 24 hours.
Compositions of the present invention may also preferably be prepared by a method which comprises:
(a) dissolving at least 0.1, 0.5, 1, 3, 6, 12, 24 to 35 weight volume percent of gelatin, preferably recombinant gelatin, in water;
(b) adjusting the pH of the solution (a) to between 3 and 6, more preferably to between 4 and 5 and even more preferably to a pH of 4.5;
(c) cross-linking the solution by adding EDC in an EDC/lysine residue, molar ratio of at least 0.6, 1.2, 3.6, 7.2, 12.5 for at least 10 minutes and up to 24 hours;
(d) ultraturaxing the cross-linked gelatin hydrogel and rinsing with water;
(e) lyophilizing the cross-linked gelatin hydrogel particles to obtain a powder.
A further aspect of the present invention provides the use of a composition comprising a cross-linked gelatin with an isoelectric point of at least 7 in the preparation of a medicament for use as a hemostatic agent. Preferences for the composition and all aspects of the gelatin and cross-linked gelatin are as described above.
The hemostatic agent of this invention is particularly applicable to the control of bleeding from surfaces, especially large surfaces. For example, the hemostatic agent is useful on (a) a cut or severed bone, (b) a severed organ, e.g. spleen, liver or kidney which has been cut surgically or traumatically, (c) the central nervous system where small blood vessels predominate, (d) prosthetic surgery, (e) oozing surfaces resulting from the surgical removal of necrotic tissue, (f) cosmetic surgery and (g) any surfaces with oozing of blood from one or more small sources, e.g. facial cuts.
The hemostatic agent may be applied in a variety of forms, e.g. as a powder directly to the surface; as a styptic in pencil form; as a gel, a sponge or in fabric form or as a coating on a surface of a medical device, wound dressing or other medical implement. The amount of agent employed varies with the extent of the bleeding surface and severity of the blood flow. Sufficient agent is applied to effect the desired control. Every application will have its own optimal degree of cross-linking.
The invention is illustrated in the following, non-limiting examples wherein all parts and percentages are by weight unless otherwise stated.

EXAMPLES

Examples of the invention are illustrated in the accompanying figures.

FIG. 1 shows the effect of various cross-linked gelatins on the number of platelets in a blood sample;

FIG. 2 shows the level of β-thromboglobuline in a blood sample following contact with cross-linked gelatins;

FIG. 3 shows the formation of a thrombin-antithrombin complex in the presence of various cross-linked gelatins;

FIG. 4 shows blood coagulation time in the presence of various cross-linked gelatins;

FIG. 5 shows the minimum level of heparin required to prevent blood clotting in the presence of various cross-linked gelatins.

Preparation Of A Hemostatic Agent Using Different Cross Linking Methods

Recombinant gelatin CBE3 prepared as described in International Patent Application WO2008103041 was used. The cross linking procedure was as follows: CBE3 solutions (1%) were buffered at pH 4 for EDC cross linking or buffered at pH 10 for hexamethylene diisocyanate (HMDIC) or dehydrothermal treatment cross-linking (DHT) and were then freeze dried. The freeze dried CBE3 solutions were cross-linked by reacting with EDC (0.25%) or HMDIC (0.0075%) dissolved in absolute ethanol for 24 hours. At the end of the reaction ethanol was removed by a vacuum drying at room temperature. DHT cross-linking was performed by an overnight heat-treatment of freeze dried CBE3 at 80° C. followed by 8 hours at 160° C. under vacuum conditions
Assessment of Hemostatic Activity using the Dynamic Chandler loop method
The hemostatic effect of the various cross-linked gelatins was tested using the “Dynamic Chandler loop method” (Chandler AB et al. 1958, Lab Invest, 7: p110-114). This method uses hemostatic material inside a tube in a rotation mixer as a blood coagulation model. This model serves to investigate the ability of artificial surfaces to initiate the different cascade reactions of the human haemostatic system (coagulation, cell alteration, platelet and complement activation).
Blood was drawn from 3 healthy volunteers with an activated partial thromboplastin time in the normal range (age: greater than 20 and less than 40 years). The quality of the blood used for these experiments is of decisive importance. Therefore the following exclusion criteria for the blood donators were strictly fulfilled: no volunteers who smoked or had taken drugs in the previous 2 weeks, especially hemostasis-affecting agents like acetylsalicylic acid, oral contraceptives, non-steroidal antiphlogistics and others. Blood was drawn without stasis, very carefully, by venipuncture with “butterflies” (approximately, 1.4 mm) directly into sterile pre-anticoagulated containers. The anitcoagulant used was 5 IU/ml Heparin-Natrium-25000-ratiopharm (Ratiopharm GmbH, Ulm, Germany). All experiments used anticoagulant with the same lot No. Each experiment was performed in triplicate using 12.5 ml of blood from each of the three donors. The experiments were preformed at 37° C. The hemostatic agent sample added to the blood had a surface area of 50 cm². The control was blood in the absence of a cross linked gelatin.
Blood coagulation tests were carried out as follows:


Test	Evaluation
category	procedure	Determination	ELISA	Manufacturer

1. oagulation	Marker for	Thrombin-	ELISA	Dade Behring,
	Thrombin	Antithrombin III,		Schwalbach,
		complex (TAT)		Germany
2. Platelets	Number of	Blood cell	Cell	ABX
	platelets	counting	counter	Hematology,
			Micros 60	Montpellier,
				France
	Marker for	Beta-	ELISA	Diagnostica
	platelet	Thrombo-		Stago/Roche,
	activation	globuline		Mannheim,
				Germany

Results

FIG. 1

EDC cross-linked recombinant gelatin led to a reduction of blood platelets. Contact of blood with artificial surfaces leads to activation and alteration of platelets with consecutive loss of platelet functionality. A strong reduction in the amount of blood platelets is associated with a high thrombogenic potential. A significant reduction was observed in recombinant gelatin cross-linked with EDC. No reduction was observed when otherwise cross-linked.

FIG. 2

The dynamic Chandler loop experiments show that EDC cross-linked recombinant gelatin leads to activation of blood platelets. Activation of platelets by adhesion to a surface leads occurs in four steps: shape change with the formation of pseudopodia, adhesion, aggregation, and release of platelet factors out of the α-granules (platelet factor 4, R-thromboglobulin, etc.). The concentration of β-thromboglobulin in plasma corresponds with the degree of platelet activation.

FIG. 3

The dynamic Chandler loop experiments show that EDC cross-linked recombinant gelatin leads to the formation of a thrombin-antithrombin complex. Thrombin-antithrombin complex (TAT) is a sensitive marker for thrombin formation and therefore also an excellent marker for detection of coagulation activation. The TAT complex is formed after binding of generated thrombin with antithrombin-III. Extremely high TAT concentrations reflect a strong procoagulatory potency of the gelatins, particularly in an experiment with high heparin concentration (5 IU/ml).

Clotting Kinetics

FIG. 4

Clotting kinetics were measured using a coagulometer (Biomatic 2000, Sarstedt), which monitors the progress of clotting optically by measuring the absorbance of a particular wavelength of light by the sample and how it changes over time. Blood was drawn from four healthy volunteers as described above. No heparin was added to these samples. A cross-linked gelatin hemostatic agent with a surface area of 50 cm²was added to the blood. The fastest coagulation time was detected in EDC cross-linked recombinant gelatin, indicating its strong procoagulatory potency.

Example 5

Blood was drawn from donors as described in the dynamic Chandler loop experiments. Heparin-Natrium-25000-ratiopharm (Ratiopharm GmbH, Ulm, Germany) was added in a concentration of 1, 3 or 5 IU/ml to 12.5 ml blood. The blood was rotated for one hour at 37° C. with 50 cm2 of hemostatic agent sample in a Chandler loop system, after which the minimum concentration of heparin to prevent macroscopically visible thrombus formation was determined. The concentration of heparin required to prevent the formation of macroscopically visible blood clots indicates the performance of the hemostyptic agents. A heparin concentration of 1 IU/ml was necessary for the amine-amine cross-linked gelatins, whereas EDC cross-linked recombinant gelatin still provoked blood clotting at this heparin concentration. Increasing the heparin concentration to 3 UI/ml still did not inhibit blood clotting with the EDC cross-linked recombinant gelatin. The addition of 5 UI/ml heparin was necessary to prevent thrombus formation in blood to which EDC cross-linked recombinant gelatin was added.
Calculated and experimentally measured physiochemical properties of hemostatic agents prepared using different crosslinking agents.


Non	HMDIC	DHT	EDC
x-linked	x-linked	x-linked	x-linked
CBE3	CBE3	CBE3	CBE3

NH2 amount per	66	46	46	33
chain^a
COOH amount per	58	58	58	25
chain^b
Nett charge/chain	+8	−12	−12	+8
IEP theoretically	10.02*	4.67	4.67	10.22
calculated after x-
linking^c
Charge at neutral pH	+8.9	−11	−11	+8.9
Hemostatic	−	−	−	+
performance

^aThe number of free amine groups in uncross-linked and cross-linked CBE3 was chemically determined with a TNBS test (W. S. Hancock, J. E. Battersby, Anal. Biochem. 71 (1976) 260).
^bThe number of free carboxyl groups was theoretically calculated, based on the known reaction chemistry of the cross-linker
^cThe IEP was calculated assuming that all charged amino acids are equally available (no 3D structure, only linear chains)
*determined before cross-linking

Claims

1.-15. (canceled)

16. A method for hemostatic treatment, comprising administering, to a patient with bleeding, a composition comprising a cross-linked gelatin with an isoelectric point of at least 7, wherein the gelatin is a recombinant gelatin which is cross-linked using a carbodiimide and which comprises at least one RGD motif.

17. The method according to claim 16 wherein the gelatin prior to cross-linking has an isoelectric point of at least 7.

18. The method according to claim 16 wherein the gelatin prior to cross-linking has an isoelectric point of at least 9.

19. The method according to claim 16 wherein after cross-linking the cross-linked gelatin has an isoelectric point of at least 9.

20. The method according to claim 19 wherein the recombinant gelatin is free of hydroxyproline and hydroxylysine residues.

21. The method according to claim 16 wherein the recombinant gelatin comprises at least 0.40 mmol/g lysine residues before cross-linking.

22. The method according to claim 16 wherein the recombinant gelatin comprises a ratio between the total arginine and lysine amino acid residues and the total glutamine and asparagine amino acid residues that is at least 1.0.

23. The method according to claim 16 wherein the recombinant gelatin has a molecular weight of at least 50 kDa.

24. The method according to claim 16 wherein the gelatin is cross-linked using 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC).

25. The method according to claim 16 wherein the recombinant gelatin is represented by CBE3.